Collecting information
Organizing data
Beyond managing daily operations, this role is a catalyst for change-championing process engineering initiatives that maximize cost-effectiveness, streamline efficiency, and propel strategic business imperatives forward.. Continuous Improvement: Lead and participate in Lean, Six Sigma, and Kaizen initiatives to drive continuous improvement in safety, quality, and productivity.. Strong understanding of GMP, FDA regulations, and pharmaceutical manufacturing standards.. Hands-on experience with key processing technologies, including, mixing, emulsification, homogenization, liquid filling, high shear / top spray granulation, tablet compression, and film coating.. Reckitt offers eligible employees competitive benefits including medical, prescription, dental, vision, life and disability insurance; paid time off for vacation, sick, and Company recognized holidays; a 401(K) plan; generous paid parental leave; adoption and fertility support; tuition reimbursement; product discounts; and much more!
The EA Business Unit in Wendell, North Carolina, which is its U.S. headquarters, focuses on electric-vehicle charging, photovoltaic inverters, medium-voltage power distribution equipment including packaging and services, and solutions, including automation. Additionally, assembly of low-voltage motor control centers, and retrofit and replacement circuit breakers occurs at the facility. Reporting to the Senior Manufacturing Manager, The Production Manger will lead the production activities for a Siemens LV Switchboard, LV Motor Control Center, or MV Switchgear manufacturing line in Wendell, NC. You will manage the production activities, managing and reporting operational KPI's, and overseeing operational improvements. From more resource-efficient factories, resilient supply chains, and smarter buildings and grids, to sustainable transportation as well as advanced healthcare, we create technology with purpose adding real value for customers. Our Commitment to Equity and Inclusion in our Diverse Global Workforce: We value your unique identity and perspective.
We make our medicines at internal and external sites around the world and coordinate all aspects of production of Roche medicines in all disease areas and dosage forms. To ensure readiness for a step-change in the standard of care that Roche delivers in the area of Cardiovascular, Renal and Metabolism (CVRM), PT will construct a new manufacturing site in the U.S. in Holly Springs, North Carolina. As the Head of Quality Control (QC) you are initially accountable for the design, qualification and ramp-up of the green field high volume facility's QC operations, including strategic workforce planning, hiring the respective personnel, setting up the organization, all relevant processes and documentation (e.g. SOPs). You are responsible for ensuring timely ramp-up including the project management activities, IT systems and definition of the processes in compliance with GMP/Quality requirements. You will transition to local full time on-site work once the site buildings are built and equipment delivered.
Join our innovative team as an Industrial Maintenance Electrician.. This overnight position offers a 2-3-2 schedule from 6 pm to 6 am, with every other weekend off.. Previous experience in a food manufacturing environment is preferred.. About Us: At Kellanova, we aim to be the leading snacks-led powerhouse, leveraging our iconic brands and passionate people.. We value equity, diversity, and inclusion, ensuring all employees have a voice and a place in our team.
In this hybrid position, you will work with our local and international team to deliver top-quality projects to our customers in the Pharmaceutical Manufacturing environment.. In systems of production-related IT/OT (MES/MOM) you map production processes and apply relevant industrial standards (ISA95, OPC UA, etc.. You implement production management systems (MES/MOM) for our customers and support their integration into enterprise resource planning systems (L4) or shop floor systems (L2). You have solid experience in the OT environment (MES) in Pharmaceutical, Biotech, or Life Sciences industries, ideally with first project management experience. Knowledge in process consulting/optimization and requirements engineering as well as in vertical MES integration (ERP, automation, LIMS, logistics) is an advantage
Beyond managing daily operations, this role is a catalyst for change—championing process engineering initiatives that maximize cost-effectiveness, streamline efficiency, and propel strategic business imperatives forward.. Continuous Improvement: Lead and participate in Lean, Six Sigma, and Kaizen initiatives to drive continuous improvement in safety, quality, and productivity.. Strong understanding of GMP, FDA regulations, and pharmaceutical manufacturing standards.. Hands-on experience with key processing technologies, including, mixing, emulsification, homogenization, liquid filling, high shear / top spray granulation, tablet compression, and film coating.. Reckitt offers eligible employees competitive benefits including medical, prescription, dental, vision, life and disability insurance; paid time off for vacation, sick, and Company recognized holidays; a 401(K) plan; generous paid parental leave; adoption and fertility support; tuition reimbursement; product discounts; and much more!
This role oversees all aspects of production, maintenance, tooling, shipping, and warehousing, while promoting a motivating environment based on trust, respect, and organizational values.. Foster a strong culture of continuous improvement through the application of lean manufacturing principles.. Collaborate with production control teams to develop schedules and meet on-time delivery goals.. Monitor and reduce scrap rates and identify trends for improvement.. Proven experience leading and implementing Lean manufacturing methodologies, including pull systems.
We make our medicines at 9 sites around the world and coordinates all aspects of production of Roche medicines in all disease areas and dosage formsTo ensure readiness for a step-change in the standard of care that Roche delivers in the area of Cardiovascular, Renal and Metabolism (CVRM), PTM will construct a new manufacturing site in the U.S. in Holly Spring, North Carolina. The new site will focus on large volume low cost Drug Product manufacturing (Component Prep & Compounding, Liquid PFS Filling, Automated Inspection, Autoinjector Assembly, Packaging/Finished Products). The Opportunity:As the Senior/Executive Director, Manufacturing you are initially accountable for the design, qualification and ramp-up of the green field high volume facility’s Compounding, Filling, and Inspection operations, including strategic workforce planning, hiring the respective personnel, setting up the organization, all relevant processes and documents/documentation (e.g. SOPs and batch documentation). You are responsible for ensuring timely ramp-up including the project management activities, IT systems and definition of the specifications and processes in compliance with GMP/Quality requirements. You will transition to local full time on-site work once the site buildings are built and equipment delivered.
Bachelor of Science (BS) in packaging/ mechanical/ chemical/ biochemical engineering, pharmaceutical science or chemistry or related fields with fifteen (15) years relevant experience pharmaceutical packaging, combination product assembly and packaging, or related technical fields;. Master of Science (MS) in packaging/ mechanical/ chemical/ biochemical engineering, pharmaceutical science or chemistry or related fields with twelve (12) years relevant experience pharmaceutical packaging, combination product assembly and packaging, or related technical fields;. PhD in packaging/ mechanical/ chemical/ biochemical engineering, pharmaceutical science or chemistry or related fields with eight (8) years relevant experience pharmaceutical packaging, combination product assembly and packaging, or related technical fields. Demonstrated depth in commercialization and tech transfer, assembly and packaging process improvement and support from early stage through launch and supply, including components, process, and equipment, as well as qualification and validation.. + Strong strategic and analytical thinking, with a focus on driving continuous improvement and implementing best practices in technical support and product stewardship.
Caterpillar is seeking a Production Manager in Clayton, NC. In this role, you will be responsible for managing production, team members and overall performance of designated value stream.. The job role may be supervising either assembly or logistics warehousing operations.. Responsibilities include meeting Caterpillar's goals for People, Quality, Velocity and Cost. Daily tie-in with production management to designate work load, priorities and sequence for work assigned. Implement various corporate initiatives such as 5S, Lean Manufacturing, 6 Sigma, CQMS/ISO certification, etc
In this hybrid position, you will work with our local and international team to deliver top-quality projects to our customers in the Pharmaceutical Manufacturing environment.. In systems of production-related IT/OT (MES/MOM) you map production processes and apply relevant industrial standards (ISA95, OPC UA, etc.). You implement production management systems (MES/MOM) for our customers and support their integration into enterprise resource planning systems (L4) or shop floor systems (L2). You have solid experience in the OT environment (MES) in Pharmaceutical, Biotech, or Life Sciences industries, ideally with first project management experience. Knowledge in process consulting/optimization and requirements engineering as well as in vertical MES integration (ERP, automation, LIMS, logistics) is an advantage
Automation Controls Technician| Raleigh | HIRING IMMEDIATELY. Integrated healthcare programs – telemedicine, chronic condition, weight management and msk health. Technical Degree - Industrial Automation. 3- 5 years’ automation technician experience. The Evergreen Packaging Raleigh Carton Converting Facility is located in Raleigh, North Carolina, which is also home to North Carolina State University and the state's capitol.
With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year.. In this vital role you will communicate and interface between the GMP manufacturing teams in the Amgen North Carolina (ANC) Biologics Drug Substance Manufacturing plant and Process Development scientific groups.. It is a highly visible role across the site with the core responsibility of hosting cross-functional meetings to drive to timelines to support the tech transfer of the program into the facility as well as process ownership for some upstream process unit operations.. New Product Introduction (NPI) lead coordinating with Manufacturing, Process Development, Supply Chain, Planning, Facilities and Engineering, as well as Quality to introduce new Drug Substance products and/or advanced technologies into the plant using project management tools (i.e. Smartsheet).. Strong technical knowledge of Upstream drug substance processing (media preparation, cell culture, harvest) and a broad understanding of related disciplinary areas in bioprocessing.
Manage Maintenance resources, equipment, and materials to support plant operations by implementing capital projects aimed to advance the manufacturing process by reducing cost, waste and improve efficiency, quality, and safety.. Promotes a strong safety culture and demonstrates adherence to all Environmental, Health and Safety policies and procedures. Knowledge of CMMS (Computerized Maintenance Management System) and P.M. (preventive maintenance) practices. Have computer literacy to be able to use CMMS, electronic mail communication, spreadsheets, and word processing.. Ability to push and pull with the arms and body to move items on two-wheeled dolly, four-wheeled cart, and hydraulic pallet jack.
Join a collaborative, fast‑paced laboratory contributing to impactful research through hands‑on work in primary cell culture, organ perfusion, and lab operations.. Characterize cells using flow cytometry, immunophenotyping, and cell-based assays.. Entry-level to mid-level experience in primary cell culture, organ perfusion, or tissue processing is appropriate depending on seniority.. Experience in flow cytometry workflows: instrument operation, panel design, QC, and data analysis.. Competence in assay development and execution (cell-based assays, immunoassays, viability or differentiation assays).
As Director of Warehouse & Logistics, you will own and lead the consolidation of warehouse operations from multiple divisional sites into a centralized, efficient hub-and-spoke model.. Lead the immediate optimization of warehousing operations while planning the phased evolution of logistics functions. Develop and implement performance metrics aligned with corporate strategy to drive continuous improvement. Standardize inventory control, warehouse workflows, and delivery processes including picking and kitting. Proven expertise with Warehouse Management Systems (WMS), specifically Zebra
Candidate must be located within commuting distance of Richardson, TX/ Raleigh, NC/ Indianapolis, IN/ Hartford, CT/Tempe, AZ or be willing to relocate to the area.. Functional domains – Vehicle order Planning & production Scheduling, Vehicle Logistics, Distribution center management, Supplier Visibility, Dynamic Order Management, warehouse management, Automotive sales and aftersales, Production management, Automotive digital retail, Auto finance.. Any relevant certification will be an added advantage – Six Sigma, APICS, SCOR, PMP etc.. Implementation / Working Knowledge of SCM packages such as SAP Ariba, Kinaxis, Blue Yonder, Oracle etc. Exposure of working in Automotive sales and aftersales, Production management, Automotive digital retail, Auto finance
Asset management, customer growth and maintenance, revenue production, personnel development and inventory control are key result areas of this position. The Big 5 is done daily. Reports directly to the Regional Manager.. Assist with completion of quality control calls on all new lease agreements within 1 business day of delivery.. Assist with physically monitoring the back door whenever inventory movement occurs
Growing stable manufacturer needs someone to supervise 4 technicians in the maintenance department overseeing facilities, equipment in the plant.. Will develop maintenance schedules for production/packaging equipment including blenders, HVAC, packaging equipment, gearboxes, and motors.. Will maintain proper inventory for spare parts, utilize PM software, assist with repairs when an emergency occurs to keep the plant running, and assure that the facilities are kept in a clean condition.. Position will require 10+ years experience with maintenance supervision in a food, cosmetic, chemical, or related industry.. Spanish language skills is a plus.
Regulatory scope will include but is not limited to applicable instruments like in ovo, in vivo, in vitro devices, analyzers, microscopes, and centrifuges.. Identify and interpret hardware safety, EMC, and environmental standards (e.g., ISO, IEC, FDA, ASME) for product compliance.. Strong knowledge of product development lifecycle, reliability engineering, and risk management tools.. Proficiency with control loop systems and engineering drawing/document management systems (EDM, EPDM, PLM, SAP).. Advanced data analytics skills using MiniTab, JMP, Python, SQL, and spreadsheets.